Department of Horticulture, Michigan State University, East Lansing, MI 48824-1222, USA.
Plant Mol Biol. 2012 Mar;78(4-5):489-501. doi: 10.1007/s11103-012-9880-7. Epub 2012 Jan 21.
While many aspects of primary cell wall have been extensively elucidated, our current understanding of secondary wall biosynthesis is limited. Recently, transcription factor MYB46 has been identified as a master regulator of secondary wall biosynthesis in Arabidopsis thaliana. To gain better understanding of this MYB46-mediated transcriptional regulation, we analyzed the promoter region of a direct target gene, AtC3H14, of MYB46 and identified a cis-acting regulatory motif that is recognized by MYB46. This MYB46-responsive cis-regulatory element (M46RE) was further characterized and shown to have an eight-nucleotide core motif, RKTWGGTR. We used electrophoretic mobility shift assay, transient transcriptional activation assay and chromatin immunoprecipitation analysis to show that the M46RE was necessary and sufficient for MYB46-responsive transcription. Genome-wide analysis identified that the frequency of M46RE in the promoters were highly enriched among the genes upregulated by MYB46, especially in the group of genes involved in secondary wall biosynthesis.
尽管人们已经对初生细胞壁的许多方面进行了广泛的阐述,但我们对次生细胞壁生物合成的理解还很有限。最近,转录因子 MYB46 被鉴定为拟南芥次生细胞壁生物合成的主要调控因子。为了更好地理解这种由 MYB46 介导的转录调控,我们分析了 MYB46 的一个直接靶基因 AtC3H14 的启动子区域,并鉴定出一个由 MYB46 识别的顺式作用调节基序。这个 MYB46 反应性顺式调控元件(M46RE)进一步被表征,并显示出具有八核苷酸核心基序 RKTWGGTR。我们使用电泳迁移率变动分析、瞬时转录激活分析和染色质免疫沉淀分析表明,M46RE 对于 MYB46 反应性转录是必要且充分的。全基因组分析表明,在 MYB46 上调的基因的启动子中,M46RE 的频率高度富集,尤其是在参与次生细胞壁生物合成的基因组中。